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分析影响斑块状银屑病患者接受甲氨蝶呤单药治疗时目标 PASI 反应和不良反应的因素:一项多中心 1521 例患者的研究。

Analysis of factors influencing target PASI responses and side effects of methotrexate monotherapy in plaque psoriasis: a multicenter study of 1521 patients.

机构信息

Department of Dermatology TR, Ankara Bilkent City Hospital, Ankara, Türkiye.

Department of Dermatology TR, Ankara Yıldırım Beyazıt University, Ankara, Türkiye.

出版信息

Arch Dermatol Res. 2024 May 25;316(6):278. doi: 10.1007/s00403-024-03066-1.

Abstract

Methotrexate (MTX) is commonly used as first-line systemic treatment agent in psoriasis. We aimed to evaluate the clinical characteristics and treatment responses of patients with psoriasis undergoing MTX monotherapy. Data from adult patients with plaque psoriasis who received MTX monotherapy for at least 3 months between April 2012 and April 2022 were retrospectively evaluated in 19 tertiary care centers. Our study included 722 female and 799 male patients, a total of 1521 participants. The average age of the patients was 44.3 ± 15.5 years. Mode of treatment was oral in 20.4% of patients while in 79.4% it was subcutaneous. The median treatment duration was 8 months (IQR = 5-15). The median weekly dose was 15 mg (IQR = 11-15). 1448 (95.2%) patients were taking folic acid supplementation. At week 12, 16.3% of the patients achieved PASI (Psoriasis Area and Severity Index) 90 response while at week 24, 37.3% achieved it. Logistic regression analysis for week 12 identified the following independent factors affecting PASI 90 achievement positively: median weekly MTX dose ≤ 15 mg (P = 0.011), subcutaneous administration (P = 0.005), no prior systemic treatment (< 0.001) and folic acid use (0.021). In logistic regression analysis for week 24; median weekly MTX dose ≤ 15 mg (P = 0.001), baseline PASI ≥ 10 (P < 0.001), no prior systemic treatment (P < 0.004), folic acid use (P = 0.001) and absence of comorbidities (P = 0.009) were determined as independent factors affecting the achievement of PASI 90. Adverse effects were observed in 38.8% of the patients, with nausea/vomiting (23.9%) and transaminase elevation (13%) being the most common. The most common reasons for interruptions (15.3%) and discontinuations (27.1%) of the treatment were patient related individual factors. The use of MTX as the first systemic treatment agent, at doses ≤ 15 mg/week and concurrent folic acid application are positive predictive factors for achieving the target PASI response both at weeks 12 and 24. In our study, which is one of the most comprehensive studies on MTX treatment in psoriasis, we observed that MTX is an effective and safe treatment option.

摘要

甲氨蝶呤(MTX)通常作为银屑病的一线全身治疗药物。我们旨在评估接受 MTX 单药治疗的银屑病患者的临床特征和治疗反应。在 19 个三级护理中心,对 2012 年 4 月至 2022 年 4 月期间接受 MTX 单药治疗至少 3 个月的成年斑块状银屑病患者的数据进行了回顾性评估。我们的研究包括 722 名女性和 799 名男性,共计 1521 名参与者。患者的平均年龄为 44.3±15.5 岁。20.4%的患者采用口服治疗,79.4%的患者采用皮下治疗。中位治疗持续时间为 8 个月(IQR=5-15)。中位每周剂量为 15mg(IQR=11-15)。1448 名(95.2%)患者正在服用叶酸补充剂。在第 12 周时,16.3%的患者达到 PASI(银屑病面积和严重程度指数)90 缓解,而在第 24 周时,37.3%的患者达到了该缓解。第 12 周时,影响 PASI 90 缓解的独立因素的逻辑回归分析表明:中位每周 MTX 剂量≤15mg(P=0.011)、皮下给药(P=0.005)、无既往全身治疗(<0.001)和叶酸使用(0.021)。第 24 周时,影响 PASI 90 缓解的独立因素的逻辑回归分析表明:中位每周 MTX 剂量≤15mg(P=0.001)、基线 PASI≥10(P<0.001)、无既往全身治疗(P<0.004)、叶酸使用(P=0.001)和无合并症(P=0.009)。38.8%的患者出现不良反应,最常见的是恶心/呕吐(23.9%)和转氨酶升高(13%)。治疗中断(15.3%)和停止(27.1%)的最常见原因是与患者相关的个体因素。每周剂量≤15mg 且同时使用叶酸的 MTX 作为一线全身治疗药物是在第 12 周和第 24 周达到目标 PASI 缓解的阳性预测因素。在我们的研究中,MTX 是一种有效的安全治疗选择,是银屑病的一线全身治疗药物。我们观察到 MTX 是一种有效的安全治疗选择。

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